Examples of 'trifluoromethoxy' in a sentence
Meaning of "trifluoromethoxy"
Trifluoromethoxy is a chemical term describing a molecule with three fluorine atoms and one methoxy (O-CH3) group
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- The univalent radical CF₃O- derived from methoxy
How to use "trifluoromethoxy" in a sentence
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trifluoromethoxy
Particular haloalkoxy group are trifluoromethoxy and trifluoroethoxy.
The trifluoromethoxy group is especially preferred.
Particular haloalkoxy groups are trifluoromethoxy and trifluoroethoxy.
Haloalkyl is typically trifluoromethyl and haloalkoxy is typically trifluoromethoxy.
Exemplary haloalkyl groups include trifluoromethoxy and difluoromethoxy.
A preferred perhalogenated alkyl group is for example trifluoromethyl or trifluoromethoxy.
Preferred haloalkoxy are trifluoromethoxy and trifluoroethoxy.
Specific examples are difluoromethoxy and trifluoromethoxy.
Among them, trifluoromethyl and trifluoromethoxy are recited as specifically preferable examples.
The polyfluoroalkoxy radicals are preferably trifluoromethoxy radicals.
The fluoromethoxy, difluoromethoxy and trifluoromethoxy groups are most preferred, especially the trifluoromethoxy group.
An example ofa haloalkoxy group is trifluoromethoxy.
The term trifluoromethoxy refers to the moiety CF3O -.
More particular haloalkoxy group is trifluoromethoxy.
The term trifluoromethoxy refers to the following substituent - OCF ₃.
See also
trifluoromethanesulfonic acid
trifluoromethanesulfonic anhydride
trifluoromethyl
trifluoromethyl group
trifluoromethanesulfonic anhydride
trifluoromethyl
trifluoromethyl group
Specific groups are difluoromethoxy and trifluoromethoxy.
Represents halogen, cyano, trifluoromethyl, trifluoromethoxy or difluoromethoxy ; R4 represents hydrogen or methyl ;.
Examples of haloalkoxy groups include difluoromethoxy and trifluoromethoxy.
For example, there may be mentioned a trifluoromethoxy group and a trifluoroethoxy group.
Examples of substituted alkyl and substituted alkoxy are trifluoromethyl and trifluoromethoxy.
More preferably it is a trifluoromethoxy group.
Haloalkyl and haloalkoxy are especially trifluoromethyl, pentafluoroethyl and trifluoromethoxy.
For example, trifluoromethyl and trifluoromethoxy are included.
Similarly, an example of a haloalkoxy group is a perhalogenated group, such as trifluoromethoxy.
Particular haloalkoxy groups are trifluoromethoxy and 2,2-difluoroethoxy.
Representative lower haloalkoxy groups are difluoromethoxy, trifluoromethoxy.
Examples of such radicals include fluoromethoxy, chloromethoxy, trifluoromethoxy ( -OCF3 ), trifluoroethoxy, fluoroethoxy, fluoropropoxy and cyclopropylmethoxy.
The above haloalkoxy group is specifically exemprified by trifluoromethoxy group.
Non-limiting examples of perfluoroalkoxy substituents include trifluoromethoxy ( -O-CF3 ), perfluoroisopropoxy, perfluorobutoxy, perfluorodecoxy, and perfluorododecoxy.
A preferred example of haloalkoxy is trifluoromethoxy.
In an embodiment, R2 is trifluoromethoxy and C * is a stereocenter with a ( R ) configuration.
A preferred haloalkoxy group is trifluoromethoxy.
Suitable examples of specific substituents on Z include methyl, difluoroazetidinyl, methoxy, ethoxy, isopropoxy, difluoromethoxy and trifluoromethoxy.
It may be in particular a trifluoromethoxy group.
Preferred haloalkoxy groups include fluoroalkoyls, such as fluoromethoxy, difluoromethoxy, trifluoromethoxy.
Most preferred is trifluoromethoxy.
Examples of the halogenomethoxy group include fluoromethoxy, difluoromethoxy, and trifluoromethoxy.
For example, methoxy, ethoxy, isopropoxy, tert-butoxy, trifluoromethoxy and the like can be mentioned.
The optional substituents include monohalo and dihalo, trifluoromethyl and trifluoromethoxy.
A typical haloalkoxy is trifluoromethoxy.
Preferred R8 is selected from chloro, methyl, methoxy, methylthio, monofluoromethyl, difluoromethyl, trifluoromethyl, monofluoromethoxy, difluoromethoxy, and trifluoromethoxy.
A preferred example is trifluoromethoxy.
Preferably, such a terminal fluorine-substituted alkoxy group is trifluoromethoxy.
Preferred haloalkoxy is trifluoromethoxy.
Particularly preferred examples of the halogenoalkoxy group include fluoromethoxy group, difluoromethoxy group and trifluoromethoxy group.
Examples of such groups include difluoromethoxy or trifluoromethoxy and the like.
R1 can be methoxy or substituted methoxy, for example fluoromethoxy, difluoromethoxy or trifluoromethoxy.
Represents halogen, cyano, trifluoromethyl, trifluoromethoxy or difluoromethoxy ;.
Where R3 is a haloalkoxy, suitable haloalkoxy groups include halomethoxy, in particular trifluoromethoxy.
Particularly preferred is trifluoromethoxy.
